# tetracycline hydrochloride

NDC: 23155-017
Generic name: tetracycline hydrochloride
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240915

FDA application: NDA050278

## Active ingredients

- TETRACYCLINE HYDROCHLORIDE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-017"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-017
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eaa5b1bd-0927-46e4-b941-32fcc492d258